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Updated: Nov 1, 2025

Flow Cytometry-Based Isolation and Therapeutic Evaluation of Tumor-Infiltrating Lymphocytes in a Mouse Model of Pancreatic Cancer
Published on: January 17, 2025
Cancer environmental immunotherapy: starving tumor cell to death by targeting TGFB on immune cell
Xing Huang1,2, Gang Zhang3,2, Tingbo Liang1,2
1Department of Hepatobiliary and Pancreatic Surgery, the First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China dr.huangxing@foxmail.com liangtingbo@zju.edu.cn.
Abstract:
The blockage of intersectional communication between tumor and its metabolic and immune microenvironment is now considered a promising solution in treating cancer. Tumors have been identified as a special type of "wounds" that do not heal. Recent studies demonstrate that the lack of the transforming growth factor beta (TGFB) signaling pathway in CD4+ helper T cells induces the remodeling of the intratumoral vascular tissue, like healing "wounds" in damaged tissues caused by tumor overgrowth, which consequently prevents tumor cells from receiving the required nutrients in their microenvironment. TGFB blockade thereby promotes damaged tissue healing, causing tumor cell death as a result of starvation, ultimately obtaining an effective anticancer immunotherapy immune response. Here, we comment on the TGFB-mediated crosstalk between immune system and nutritional supply, highlighting cancer immunotherapeutic strategies targeting environmental immune-metabolism interplay. Cancer environmental immunotherapy targeting TGFB might therefore become one of the most promising treatment strategies for patients with cancer.
Insights
Blocking transforming growth factor beta (TGFB) signaling in T cells can prevent tumors from accessing nutrients, leading to cancer cell death. This approach shows promise for effective cancer immunotherapy by targeting the tumor
Area of Science:
- Cancer Biology
- Immunology
- Metabolic Research
Background:
- Tumors are characterized as non-healing wounds, disrupting their microenvironment.
- Intersectional communication between tumors and their metabolic/immune surroundings is crucial for cancer progression.
- The transforming growth factor beta (TGFB) signaling pathway plays a significant role in this interplay.
Purpose of the Study:
- To comment on TGFB-mediated crosstalk between the immune system and nutritional supply in cancer.
- To highlight cancer immunotherapeutic strategies targeting the immune-metabolism interplay within the tumor microenvironment.
- To explore the potential of TGFB blockade as a novel cancer treatment.
Main Methods:
- Analysis of recent studies on TGFB signaling in CD4+ helper T cells.
- Investigation of the effects of TGFB pathway blockade on intratumoral vascular remodeling.
- Commentary on the impact of nutrient deprivation on tumor cells.
Main Results:
- Lack of TGFB signaling in CD4+ T cells induces vascular remodeling, mimicking wound healing.
- This remodeling prevents tumor cells from receiving essential nutrients, leading to starvation.
- TGFB blockade promotes an effective anti-cancer immune response.
Conclusions:
- Targeting TGFB in cancer immunotherapy offers a promising strategy by disrupting tumor nutrient supply.
- Exploiting the immune-metabolism interplay via TGFB blockade could lead to effective cancer treatments.
- Cancer environmental immunotherapy targeting TGFB represents a potentially groundbreaking approach for patients.
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